-
1
-
-
10844232112
-
Whole genome DNA copy number changes identified by high density oligonucleotide arrays
-
Huang J, Wei W, Zhang J, Liu G, Bignell GR, Stratton MR, et al. Whole genome DNA copy number changes identified by high density oligonucleotide arrays. Hum Genomics 2004, 1:287-299.
-
(2004)
Hum Genomics
, vol.1
, pp. 287-299
-
-
Huang, J.1
Wei, W.2
Zhang, J.3
Liu, G.4
Bignell, G.R.5
Stratton, M.R.6
-
2
-
-
10744230160
-
High-resolution analysis of DNA copy number using oligonucleotide microarrays
-
10.1101/gr.2012304, 327104, 14762065
-
Bignell GR, Huang J, Greshock J, Watt S, Butler A, West S, et al. High-resolution analysis of DNA copy number using oligonucleotide microarrays. Genome Res 2004, 14:287-295. 10.1101/gr.2012304, 327104, 14762065.
-
(2004)
Genome Res
, vol.14
, pp. 287-295
-
-
Bignell, G.R.1
Huang, J.2
Greshock, J.3
Watt, S.4
Butler, A.5
West, S.6
-
3
-
-
25444510786
-
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event
-
10.1158/0008-5472.CAN-05-0842, 16204023
-
Teh MT, Blaydon D, Chaplin T, Foot NJ, Skoulakis S, Raghavan M, et al. Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event. Cancer Res 2005, 65:8597-8603. 10.1158/0008-5472.CAN-05-0842, 16204023.
-
(2005)
Cancer Res
, vol.65
, pp. 8597-8603
-
-
Teh, M.T.1
Blaydon, D.2
Chaplin, T.3
Foot, N.J.4
Skoulakis, S.5
Raghavan, M.6
-
4
-
-
27144478643
-
Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias
-
10.1158/0008-5472.CAN-05-2017, 16230371
-
Fitzgibbon J, Smith LL, Raghavan M, Smith ML, Debernardi S, Skoulakis S, et al. Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias. Cancer Res 2005, 65:9152-9154. 10.1158/0008-5472.CAN-05-2017, 16230371.
-
(2005)
Cancer Res
, vol.65
, pp. 9152-9154
-
-
Fitzgibbon, J.1
Smith, L.L.2
Raghavan, M.3
Smith, M.L.4
Debernardi, S.5
Skoulakis, S.6
-
5
-
-
12544257171
-
Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias
-
Raghavan M, Lillington DM, Skoulakis S, Debernardi S, Chaplin T, Foot NJ, et al. Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias. Cancer Res 2005, 65:375-378.
-
(2005)
Cancer Res
, vol.65
, pp. 375-378
-
-
Raghavan, M.1
Lillington, D.M.2
Skoulakis, S.3
Debernardi, S.4
Chaplin, T.5
Foot, N.J.6
-
6
-
-
33644906665
-
Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma
-
10.1002/gcc.20262, 16149064
-
Langdon JA, Lamont JM, Scott DK, Dyer S, Prebble E, Bown N, et al. Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma. Genes Chromosomes Cancer 2006, 45:47-60. 10.1002/gcc.20262, 16149064.
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 47-60
-
-
Langdon, J.A.1
Lamont, J.M.2
Scott, D.K.3
Dyer, S.4
Prebble, E.5
Bown, N.6
-
7
-
-
34047258036
-
Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays
-
10.1158/0008-5472.CAN-06-4152, 17363583
-
Stark M, Hayward N. Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays. Cancer Res 2007, 67:2632-2642. 10.1158/0008-5472.CAN-06-4152, 17363583.
-
(2007)
Cancer Res
, vol.67
, pp. 2632-2642
-
-
Stark, M.1
Hayward, N.2
-
8
-
-
34548064529
-
Comprehensive analysis of copy number and allele status identifies multiple chromosome defects underlying follicular lymphoma pathogenesis
-
10.1158/1078-0432.CCR-07-0456, 17699855
-
Ross CW, Ouillette PD, Saddler CM, Shedden KA, Malek SN. Comprehensive analysis of copy number and allele status identifies multiple chromosome defects underlying follicular lymphoma pathogenesis. Clin Cancer Res 2007, 13:4777-4785. 10.1158/1078-0432.CCR-07-0456, 17699855.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 4777-4785
-
-
Ross, C.W.1
Ouillette, P.D.2
Saddler, C.M.3
Shedden, K.A.4
Malek, S.N.5
-
9
-
-
33645736791
-
Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers
-
10.1158/0008-5472.CAN-05-3285, 16585170
-
Gaasenbeek M, Howarth K, Rowan AJ, Gorman PA, Jones A, Chaplin T, et al. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers. Cancer Res 2006, 66:3471-3479. 10.1158/0008-5472.CAN-05-3285, 16585170.
-
(2006)
Cancer Res
, vol.66
, pp. 3471-3479
-
-
Gaasenbeek, M.1
Howarth, K.2
Rowan, A.J.3
Gorman, P.A.4
Jones, A.5
Chaplin, T.6
-
10
-
-
33845652312
-
Frequent occurrence of uniparental disomy in colorectal cancer
-
10.1093/carcin/bgl086, 16774939
-
Andersen CL, Wiuf C, Kruhoffer M, Korsgaard M, Laurberg S, Orntoft TF. Frequent occurrence of uniparental disomy in colorectal cancer. Carcinogenesis 2007, 28:38-48. 10.1093/carcin/bgl086, 16774939.
-
(2007)
Carcinogenesis
, vol.28
, pp. 38-48
-
-
Andersen, C.L.1
Wiuf, C.2
Kruhoffer, M.3
Korsgaard, M.4
Laurberg, S.5
Orntoft, T.F.6
-
11
-
-
55949095908
-
Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas
-
10.1007/s10689-008-9194-8, 18415027
-
van PM, Middeldorp A, Tops CM, van ER, van der Klift HM, Vasen HF, et al. Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas. Fam Cancer 2008, 7:319-330. 10.1007/s10689-008-9194-8, 18415027.
-
(2008)
Fam Cancer
, vol.7
, pp. 319-330
-
-
van, P.M.1
Middeldorp, A.2
Tops, C.M.3
van, E.R.4
van der Klift, H.M.5
Vasen, H.F.6
-
12
-
-
38549158349
-
Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization
-
10.1002/gcc.20524, 18050302
-
Lo KC, Bailey D, Burkhardt T, Gardina P, Turpaz Y, Cowell JK. Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization. Genes Chromosomes Cancer 2008, 47:221-237. 10.1002/gcc.20524, 18050302.
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 221-237
-
-
Lo, K.C.1
Bailey, D.2
Burkhardt, T.3
Gardina, P.4
Turpaz, Y.5
Cowell, J.K.6
-
13
-
-
60549097444
-
Prevalence of copy-number neutral LOH in glioblastomas revealed by genomewide analysis of laser-microdissected tissues
-
10.1215/15228517-2008-064, 2719013, 18697953
-
Kuga D, Mizoguchi M, Guan Y, Hata N, Yoshimoto K, Shono T, et al. Prevalence of copy-number neutral LOH in glioblastomas revealed by genomewide analysis of laser-microdissected tissues. Neuro Oncol 2008, 10:995-1003. 10.1215/15228517-2008-064, 2719013, 18697953.
-
(2008)
Neuro Oncol
, vol.10
, pp. 995-1003
-
-
Kuga, D.1
Mizoguchi, M.2
Guan, Y.3
Hata, N.4
Yoshimoto, K.5
Shono, T.6
-
14
-
-
34249111848
-
Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis
-
10.1002/gcc.20447, 2426828, 17420988
-
Purdie KJ, Lambert SR, Teh MT, Chaplin T, Molloy G, Raghavan M, et al. Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis. Genes Chromosomes Cancer 2007, 46:661-669. 10.1002/gcc.20447, 2426828, 17420988.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 661-669
-
-
Purdie, K.J.1
Lambert, S.R.2
Teh, M.T.3
Chaplin, T.4
Molloy, G.5
Raghavan, M.6
-
15
-
-
61849146788
-
Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations
-
10.1182/blood-2007-12-130260, 2647673, 19109227
-
Akagi T, Shih LY, Kato M, Kawamata N, Yamamoto G, Sanada M, et al. Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations. Blood 2009, 113:1741-1748. 10.1182/blood-2007-12-130260, 2647673, 19109227.
-
(2009)
Blood
, vol.113
, pp. 1741-1748
-
-
Akagi, T.1
Shih, L.Y.2
Kato, M.3
Kawamata, N.4
Yamamoto, G.5
Sanada, M.6
-
16
-
-
59449093453
-
A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups
-
10.1182/blood-2008-07-166801, 18838613
-
Sulong S, Moorman AV, Irving JA, Strefford JC, Konn ZJ, Case MC, et al. A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups. Blood 2009, 113:100-107. 10.1182/blood-2008-07-166801, 18838613.
-
(2009)
Blood
, vol.113
, pp. 100-107
-
-
Sulong, S.1
Moorman, A.V.2
Irving, J.A.3
Strefford, J.C.4
Konn, Z.J.5
Case, M.C.6
-
17
-
-
70349334416
-
Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis
-
10.1002/gcc.20694, 19603523
-
Gorringe KL, Ramakrishna M, Williams LH, Sridhar A, Boyle SE, Bearfoot JL, et al. Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis. Genes Chromosomes Cancer 2009, 48:931-942. 10.1002/gcc.20694, 19603523.
-
(2009)
Genes Chromosomes Cancer
, vol.48
, pp. 931-942
-
-
Gorringe, K.L.1
Ramakrishna, M.2
Williams, L.H.3
Sridhar, A.4
Boyle, S.E.5
Bearfoot, J.L.6
-
18
-
-
49249119361
-
Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays
-
10.1158/0008-5472.CAN-07-6710, 18519675
-
Nancarrow DJ, Handoko HY, Smithers BM, Gotley DC, Drew PA, Watson DI, et al. Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays. Cancer Res 2008, 68:4163-4172. 10.1158/0008-5472.CAN-07-6710, 18519675.
-
(2008)
Cancer Res
, vol.68
, pp. 4163-4172
-
-
Nancarrow, D.J.1
Handoko, H.Y.2
Smithers, B.M.3
Gotley, D.C.4
Drew, P.A.5
Watson, D.I.6
-
19
-
-
77950990572
-
Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies
-
10.1182/blood-2009-10-201848, 20107230
-
O'Keefe C, McDevitt MA, Maciejewski JP. Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies. Blood 2010, 115:2731-2739. 10.1182/blood-2009-10-201848, 20107230.
-
(2010)
Blood
, vol.115
, pp. 2731-2739
-
-
O'Keefe, C.1
McDevitt, M.A.2
Maciejewski, J.P.3
-
20
-
-
0020331835
-
Epidemiology of esophageal cancer in China
-
Li JY. Epidemiology of esophageal cancer in China. Natl Cancer Inst Monogr 1982, 62:113-120.
-
(1982)
Natl Cancer Inst Monogr
, vol.62
, pp. 113-120
-
-
Li, J.Y.1
-
21
-
-
0009545696
-
[The trends and preventive strategies of esophageal cancer in high-risk areas of Taihang Mountains, China]
-
Qiao YL, Hou J, Yang L, He YT, Liu YY, Li LD, et al. [The trends and preventive strategies of esophageal cancer in high-risk areas of Taihang Mountains, China]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao 2001, 23:10-14.
-
(2001)
Zhongguo Yi Xue Ke Xue Yuan Xue Bao
, vol.23
, pp. 10-14
-
-
Qiao, Y.L.1
Hou, J.2
Yang, L.3
He, Y.T.4
Liu, Y.Y.5
Li, L.D.6
-
22
-
-
0032712720
-
Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer
-
Hu N, Roth MJ, Emmert-Buck MR, Tang ZZ, Polymeropolous M, Wang QH, et al. Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer. Clin Cancer Res 1999, 5:3476-3482.
-
(1999)
Clin Cancer Res
, vol.5
, pp. 3476-3482
-
-
Hu, N.1
Roth, M.J.2
Emmert-Buck, M.R.3
Tang, Z.Z.4
Polymeropolous, M.5
Wang, Q.H.6
-
23
-
-
0033974187
-
Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population
-
10.1002/(SICI)1098-2264(200003)27:3<217::AID-GCC1>3.0.CO;2-A, 10679910
-
Hu N, Roth MJ, Polymeropolous M, Tang ZZ, Emmert-Buck MR, Wang QH, et al. Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population. Genes Chromosomes Cancer 2000, 27:217-228. 10.1002/(SICI)1098-2264(200003)27:3<217::AID-GCC1>3.0.CO;2-A, 10679910.
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 217-228
-
-
Hu, N.1
Roth, M.J.2
Polymeropolous, M.3
Tang, Z.Z.4
Emmert-Buck, M.R.5
Wang, Q.H.6
-
24
-
-
0033737598
-
High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China
-
10.1093/carcin/21.11.2019, 11062163
-
Huang J, Hu N, Goldstein AM, Emmert-Buck MR, Tang ZZ, Roth MJ, et al. High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China. Carcinogenesis 2000, 21:2019-2026. 10.1093/carcin/21.11.2019, 11062163.
-
(2000)
Carcinogenesis
, vol.21
, pp. 2019-2026
-
-
Huang, J.1
Hu, N.2
Goldstein, A.M.3
Emmert-Buck, M.R.4
Tang, Z.Z.5
Roth, M.J.6
-
25
-
-
25844434735
-
Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history
-
10.1002/gcc.20242, 16015646
-
Hu N, Su H, Li WJ, Giffen C, Goldstein AM, Hu Y, et al. Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history. Genes Chromosomes Cancer 2005, 44:271-278. 10.1002/gcc.20242, 16015646.
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 271-278
-
-
Hu, N.1
Su, H.2
Li, W.J.3
Giffen, C.4
Goldstein, A.M.5
Hu, Y.6
-
26
-
-
33845678584
-
Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array
-
10.1186/1471-2164-7-299, 1687196, 17134496
-
Hu N, Wang C, Hu Y, Yang HH, Kong LH, Lu N, et al. Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array. BMC Genomics 2006, 7:299. 10.1186/1471-2164-7-299, 1687196, 17134496.
-
(2006)
BMC Genomics
, vol.7
, pp. 299
-
-
Hu, N.1
Wang, C.2
Hu, Y.3
Yang, H.H.4
Kong, L.H.5
Lu, N.6
-
27
-
-
67650996833
-
Genomic characterization of esophageal squamous cell carcinoma from a high-risk population in China
-
10.1158/0008-5472.CAN-08-4622, 2734334, 19584285
-
Hu N, Wang C, Ng D, Clifford R, Yang HH, Tang ZZ, et al. Genomic characterization of esophageal squamous cell carcinoma from a high-risk population in China. Cancer Res 2009, 69:5908-5917. 10.1158/0008-5472.CAN-08-4622, 2734334, 19584285.
-
(2009)
Cancer Res
, vol.69
, pp. 5908-5917
-
-
Hu, N.1
Wang, C.2
Ng, D.3
Clifford, R.4
Yang, H.H.5
Tang, Z.Z.6
-
28
-
-
4644297556
-
Comprehensive characterization of annexin I alterations in esophageal squamous cell carcinoma
-
10.1158/1078-0432.CCR-04-0317, 15447985
-
Hu N, Flaig MJ, Su H, Shou JZ, Roth MJ, Li WJ, et al. Comprehensive characterization of annexin I alterations in esophageal squamous cell carcinoma. Clin Cancer Res 2004, 10:6013-6022. 10.1158/1078-0432.CCR-04-0317, 15447985.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 6013-6022
-
-
Hu, N.1
Flaig, M.J.2
Su, H.3
Shou, J.Z.4
Roth, M.J.5
Li, W.J.6
-
29
-
-
0034944117
-
Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinoma
-
10.1002/gcc.1158, 11433530
-
Li G, Hu N, Goldstein AM, Tang ZZ, Roth MJ, Wang QH, et al. Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinoma. Genes Chromosomes Cancer 2001, 31:390-397. 10.1002/gcc.1158, 11433530.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 390-397
-
-
Li, G.1
Hu, N.2
Goldstein, A.M.3
Tang, Z.Z.4
Roth, M.J.5
Wang, Q.H.6
-
30
-
-
0036554733
-
Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma
-
Hu N, Li G, Li WJ, Wang C, Goldstein AM, Tang ZZ, et al. Infrequent mutation in the BRCA2 gene in esophageal squamous cell carcinoma. Clin Cancer Res 2002, 8:1121-1126.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 1121-1126
-
-
Hu, N.1
Li, G.2
Li, W.J.3
Wang, C.4
Goldstein, A.M.5
Tang, Z.Z.6
-
31
-
-
50549101277
-
Replication of a genome-wide case-control study of esophageal squamous cell carcinoma
-
10.1002/ijc.23682, 2552411, 18649358
-
Ng D, Hu N, Hu Y, Wang C, Giffen C, Tang ZZ, et al. Replication of a genome-wide case-control study of esophageal squamous cell carcinoma. Int J Cancer 2008, 123:1610-1615. 10.1002/ijc.23682, 2552411, 18649358.
-
(2008)
Int J Cancer
, vol.123
, pp. 1610-1615
-
-
Ng, D.1
Hu, N.2
Hu, Y.3
Wang, C.4
Giffen, C.5
Tang, Z.Z.6
-
32
-
-
69249179575
-
Family history of cancer and risk for esophageal and gastric cancer in Shanxi, China
-
10.1186/1471-2407-9-269, 2729777, 19656375
-
Gao Y, Hu N, Han X, Giffen C, Ding T, Goldstein A, et al. Family history of cancer and risk for esophageal and gastric cancer in Shanxi, China. BMC Cancer 2009, 9:269. 10.1186/1471-2407-9-269, 2729777, 19656375.
-
(2009)
BMC Cancer
, vol.9
, pp. 269
-
-
Gao, Y.1
Hu, N.2
Han, X.3
Giffen, C.4
Ding, T.5
Goldstein, A.6
-
33
-
-
71349083223
-
Jasmine tea consumption and upper gastrointestinal cancer in China
-
Gao Y, Hu N, Han X, Giffen C, Ding T, Goldstein AM, et al. Jasmine tea consumption and upper gastrointestinal cancer in China. Cancer Causes Control 2009, 20:1997-2007.
-
(2009)
Cancer Causes Control
, vol.20
, pp. 1997-2007
-
-
Gao, Y.1
Hu, N.2
Han, X.3
Giffen, C.4
Ding, T.5
Goldstein, A.M.6
-
34
-
-
0030575911
-
Laser capture microdissection
-
10.1126/science.274.5289.998, 8875945
-
Emmert-Buck MR, Bonner RF, Smith PD, Chuaqui RF, Zhuang Z, Goldstein SR, et al. Laser capture microdissection. Science 1996, 274:998-1001. 10.1126/science.274.5289.998, 8875945.
-
(1996)
Science
, vol.274
, pp. 998-1001
-
-
Emmert-Buck, M.R.1
Bonner, R.F.2
Smith, P.D.3
Chuaqui, R.F.4
Zhuang, Z.5
Goldstein, S.R.6
-
35
-
-
0142121516
-
Exploration, normalization, and summaries of high density oligonucleotide array probe level data
-
10.1093/biostatistics/4.2.249, 12925520
-
Irizarry RA, Hobbs B, Collin F, Beazer-Barclay YD, Antonellis KJ, Scherf U, et al. Exploration, normalization, and summaries of high density oligonucleotide array probe level data. Biostatistics 2003, 4:249-264. 10.1093/biostatistics/4.2.249, 12925520.
-
(2003)
Biostatistics
, vol.4
, pp. 249-264
-
-
Irizarry, R.A.1
Hobbs, B.2
Collin, F.3
Beazer-Barclay, Y.D.4
Antonellis, K.J.5
Scherf, U.6
-
36
-
-
0037316303
-
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
-
10.1093/bioinformatics/19.2.185, 12538238
-
Bolstad BM, Irizarry RA, Astrand M, Speed TP. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics 2003, 19:185-193. 10.1093/bioinformatics/19.2.185, 12538238.
-
(2003)
Bioinformatics
, vol.19
, pp. 185-193
-
-
Bolstad, B.M.1
Irizarry, R.A.2
Astrand, M.3
Speed, T.P.4
|